Creating distortion in g-C3N4 framework by incorporation of ethylenediaminetetramethylene for enhancing photocatalytic generation of hydrogen

被引:20
作者
Su, Feng-Yun [1 ]
Zhang, Wei-De [1 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, 381 Wushan Rd, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; EDTA; Grafting; Photocatalysis; Hydrogen evolution; GRAPHITIC CARBON NITRIDE; 2-DIMENSIONAL CONJUGATED POLYMERS; VISIBLE-LIGHT; PHOTOELECTROCHEMICAL ACTIVITY; CHARGE SEPARATION; H-2; EVOLUTION; WATER; PERFORMANCE; HETEROJUNCTION; GRAPHENE;
D O I
10.1016/j.mcat.2017.02.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Relatively narrow visible light responsive region and high recombination probability of photogenerated charge carriers are the main barriers that limit the photocatalytic activity of graphitic carbon nitride (g-C3N4). In this study, modified g-C3N4 was synthesized by adding minor amount of ethylenediaminetetraacetic acid (EDTA) into urea as precursors for subsequent thermal polymerization. The thermal intermediate product ethylenediaminetetramethylene (EDTM) during decarboxylation of EDTA was grafted to the framework of g-C3N4 by connecting adjacent 3, s-triazine units. The special chelate structure of EDTA leads to the distortion of g-C3N4 to a nonplanar structure, which is responsible for extending the light harvesting around 500 nm, and consequently promoting the generation, separation and transfer of charge carriers. The H-2 evolution rate on an optimized EDTM-grafted g-C3N4 photocatalyst (UCN-10) reaches 116.4 mu mol h(-1), which is about 3.5 times of that on the pristine g-C3N4 (UCN). The formation process of the grafted structure and the mechanism for the enhanced photocatalytic H-2 evolution over UCN-10 were proposed based on experimental results. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 75
页数:12
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